NCT02043925已完成不适用
QT-prolongation in Psychiatric Hospitals
适应症
干预措施
相关药物
试验速览
- 阶段
- 不适用
- 状态
- 已完成
- 发起方
- KU Leuven
- 入组人数
- 152
- 试验地点
- 1
- 主要终点
- change in QTc-interval (corrected for heart rate)
研究概览
简要总结
Observational study in 6 psychiatric hospitals in Flanders. Patients are included when a QT-prolonging drug is added to a medication profile that already contains a potential QT-prolonging drug. An ECG is taken before the administration of the new drug and a week after starting the new drug to investigate the change in duration of the QTc-interval. Risk factors for developing QT-prolongation and blood concentrations of potassium and creatinine are documented.
研究设计
- 研究类型
- Observational
- 观察模型
- Cohort
- 时间视角
- Prospective
入排标准
- 年龄范围
- 18 Years 至 —（Adult, Older Adult）
- 性别
- All
- 接受健康志愿者
- 否
入选标准
- •inpatient in one of the 6 participating psychiatric hospitals
- •QT-prolonging drug in the medication profile and the doctor prescribes another QT-prolonging drug
排除标准
- •age < 18 year
研究组 & 干预措施
psychiatric patients treated with QT-prolonging drugs
干预措施: drugs linked with QT-prolongation (Drug)
结局指标
主要结局
change in QTc-interval (corrected for heart rate)
时间窗: before and one week after the start of a QT-prolonging drug
次要结局
未报告次要终点
研究者
研究点 (1)
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